Quality & Regulatory Staffing Solutions

We connect companies with proven Quality & Regulatory professionals who ensure safety, compliance, and innovation every step of the way.

serving the life sciences, technology, and healthcare sectors

Industry Need

Our Solution

Result

Our Expertise & Focus Areas

  • Regulatory Affairs — FDA submissions, 510(k), PMA, CE Mark, EU MDR, global regulations
  • Quality Assurance & Quality Systems — ISO 13485, CAPA, audits, QMS development
  • Validation & Verification — software, process, equipment, cleaning, sterilization
  • Clinical & Risk Management — risk files, clinical evaluations, safety documentation
  • Post-Market Surveillance & Compliance — complaint handling, vigilance, reporting

For Employers

  • Specialized RA/QA Talent with proven track records in medical devices
  • Flexible Engagement Models — consultants, contract staff, or permanent hires
  • Regulatory Insight & Guidance from candidates who’ve managed submissions and audits
  • Rapid, Targeted Delivery — talent presented in 24–72 hours
  • Support Through Audits & Inspections with experienced professionals

For Candidates

  • Access to Exclusive Opportunities in RA & QA for medical devices
  • Career Growth & Development with coaching and resume support
  • Competitive Pay & Benefits tailored to your skills and certifications
  • Work on Cutting-Edge Devices shaping the future of healthcare
  • Long-Term Career Partner — from your first contract to your next leadership role

How We Work

  • Discovery – Define regulatory/quality needs and compliance priorities
  • Targeted Sourcing – Tap into our network of RA/QA professionals
  • Seamless Placement – Fast onboarding, audit-ready talent
  • Ongoing Partnership – Continued support for both clients and candidates

Have additional quality & regulatory solutions questions?

We'd be happy to talk with you about your unique needs and goals.